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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
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- 保质期：
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- 英文名：
tert-Butyl 4-nitro-1H-indole-1-carboxylate
- 库存：
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- 供应商：
无锡云萃生物
- CAS号：
913836-24-5
- 规格：
5mg/50mg/100mg/500mg
| 规格： | 5mg | 产品价格： | ￥100.0 |
|---|---|---|---|
| 规格： | 50mg | 产品价格： | ￥100.0 |
| 规格： | 100mg | 产品价格： | ￥100.0 |
| 规格： | 500mg | 产品价格： | ￥100.0 |
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文献和实验Synthesis of Peptides Using Tert-Butyloxycarbonyl (Boc) as the -Amino Protection Group
The use of the tert -butyloxycarbonyl (Boc) as the N α-amino protecting group in peptide synthesis can be advantageous in several cases, such as synthesis of hydrophobic peptides and peptides containing ester and thioester moieties
Enzymes Acting on d-Amino Acid Containing Peptides
aminopeptidase and endopeptidase activities. The enzyme was active toward (d -Phe) n , Boc-(d -Phe) n , (d -Phe) n methyl ester, d -Phe-NH2 , Boc-(d -Phe) n methyl ester, and Boc-(d -Phe) n tert -butyl ester, but not toward (d -Ala) n (n = 2–4), (d
Methylated Polyamines as Research Tools
resulted in corresponding di-Boc-amines, which after deprotection gave target β- and γ-MeSpd’s. To prepare α-MeSpd, the starting compound, 3-amino-1-butanol, was converted into N -Cbz-3-amino-1-butyl methanesulfonate, which alkylated putrescine
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